Canonical Allele Identifier: CA1950150485

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394836C= , CM000673.2:g.6394836C=	GRCh38
NC_000011.9:g.6416066C= , CM000673.1:g.6416066C=	GRCh37
NC_000011.8:g.6372642C=	NCBI36
NG_011780.1:g.9412C=
NG_029615.1:g.29579G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.*229C= MANE Select	ENSP00000340409.4:n.*229C=
ENST00000342245.8:c.*229C=	ENSP00000340409.4:n.*229C=
ENST00000526280.1:c.1182C=
ENST00000533123.5:c.*852C=	ENSP00000435950.1:n.*852C=
ENST00000534405.5:c.*956C=	ENSP00000434353.1:n.*956C=
NM_000543.4:c.*229C=	NP_000534.3:n.*229C=
NM_001007593.2:c.*229C=	NP_001007594.2:n.*229C=
XM_011520303.1:c.*229C=	XP_011518605.1:n.*229C=
NM_001318087.1:c.*618C=	NP_001305016.1:n.*618C=
NM_001318088.1:c.*229C=	NP_001305017.1:n.*229C=
NM_001365135.1:c.*229C=	NP_001352064.1:n.*229C=
NR_027400.2:n.2138C=
NR_134502.1:n.1677C=
XR_001747940.2:n.2310C=
XR_002957158.1:n.2492C=
NM_000543.5:c.*229C= MANE Select	NP_000534.3:n.*229C=
NM_001007593.3:c.*229C=	NP_001007594.2:n.*229C=
NM_001318087.2:c.*618C=	NP_001305016.1:n.*618C=
NM_001318088.2:c.*229C=	NP_001305017.1:n.*229C=
NM_001365135.2:c.*229C=	NP_001352064.1:n.*229C=
NR_027400.3:n.2078C=
NR_134502.2:n.1617C=